Abstract
Biochar is the degradation-resistant product generated by the pyrolysis of organic materials and is produced for the intended use of land application in order to promote carbon sequestration and soil improvement. However, despite the many potential benefits biochar application offers, it is important to quantify any ecological impacts that may result from soil amendment in order to avoid potentially causing negative effects upon soil biota which are crucial in the many ecosystem services provided by soil. Any impacts on earthworms in particular are important to evaluate because of their pivotal role in organic matter breakdown, nutrient cycling and soil formation. In this study, we conducted a series of ecotoxicological assays to determine lethal and sublethal (avoidance, mass change and moisture content) effects of heavy biochar applications that reflect levels that may be used in soil restoration efforts. Two earthworm species, Eisenia fetida, an epigeic species, and Lumbricus terrestris, an anecic species, were utilised as test organisms. Two types of biochar, produced from wheat straw and rice husk feedstocks, respectively, were applied to OECD artificial soil and to a natural soil (Kettering loam) at rates of up to 20% w/w. The influence of biochar application on soil porewater chloride, fluoride and phosphate concentrations was also assessed. The biochar applications induced only a subtle level of avoidance behaviour while effects on survival over a 4-week exposure period were inconsistent. However, death and physical damage to some individual earthworms at high biochar application rates were observed, the mechanisms and processes leading to which should be investigated further. Earthworm development (mean mass change over time) proved to be a more sensitive measure, revealing negative effects on L. terrestris at 10% and 20% (w/w) wheat biochar applications in OECD soil and at 20% (w/w) applications of both biochars in Kettering loam. The moisture content of E. fetida remained remarkably consistent across all treatments (~ 82%), indicating that this is not a sensitive measure of effects. The high rates of biochar application resulted in increased chloride (2 to 3-fold) and phosphate (100-fold) concentrations in simulated soil porewaters, which has important implications for soil fertility and production but also for environmental management.
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Introduction
Biochar is the carbonaceous residue created during the pyrolysis, i.e. thermal decomposition, of biomass under low oxygen conditions (Lehmann and Joseph 2009) and is being increasingly produced and incorporated into soil because of its potential to sequester carbon and thus mitigate climate change through increasing the long-term storage of carbon in soils (e.g. McHenry 2009). Biochar applications to land are also being promoted by many voices because it can additionally offer a host of other benefits to soils; such benefits may include increasing the recalcitrant organic matter content of soil which consequently decreases bulk density and increases porosity, water holding capacity, hydraulic conductivity and cation exchange capacity (Huang et al. 2013). Biochar has also been identified as having potential use in remediation and restoration of degraded and contaminated soils not only because of the benefits outlined above but also because it can potentially bind, or otherwise render inactive, contaminants and toxic constituents (Beesley et al. 2011; Houben et al. 2013; Rinklebe et al. 2016). Nevertheless, the wider soil ecosystem impacts of biochar addition need to be considered and evaluated, particularly as biochar addition is effectively permanent, lasting for thousands of years, on account of its recalcitrance (Lehmann and Joseph 2009; Lone et al. 2015). The effects of biochar applications on earthworms have received very limited attention (e.g. Weyers and Spokas 2011; Malev et al. 2016) and are an important research gap considering the great importance of this organism group to soil health and ecosystem processes. Indeed, earthworms have long been recognised as ecosystem engineers, playing an essential role in organic matter decomposition, nutrient cycling, pore creation and soil formation (e.g. Darwin 1881). Moreover, earthworms are a food source for a range of mammals, birds, reptiles and amphibians, and thus, for all of these reasons, it is important to avoid causing alterations to their behaviour or to their populations in order to maintain soil and ecosystem functionality. The aim of this study, therefore, was to investigate the ecotoxicological effects of biochar addition on two earthworm species of differing ecologies, Eisenia fetida, an epigeic species, and Lumbricus terrestris, an anecic (deep burrowing) species. Lethal and sublethal endpoints were examined in order to identify a range of effects resulting from soil amendment with biochar.
Methods
Soils and biochars
The terrestrial ecotoxicology assays in this study were conducted in a natural soil, Kettering loam (Kettering, Northamptonshire, UK, supplied by Boughton Ltd., www.boughton.co.uk) and in an OECD artificial soil constructed in the laboratory. Kettering loam was selected because it is known to be suitable for a range of earthworm species and has been employed previously in multiple earthworm studies (Brinza et al. 2014; Davies et al. 2003; Langdon et al. 2003; Lowe and Butt 2005; Lowe et al. 2016). Moreover, the characteristics of Kettering loam are well established (typically pH 6.8–7.2; clay-silt-sand = 24%-18%-58%; organic content 5–7%) (Brami et al. 2017; Lowe et al. 2016). Kettering loam was dried and sieved to 2 mm prior to use. The OECD artificial soil was assembled in accordance with OECD guideline 222 (OECD 2016) and comprised ~ 70% sand obtained from Borne Amenity Ltd., Kent, UK, sieved to 2 mm, 20% kaolin clay, 10% dried sphagnum peat and a small percentage of crushed calcium carbonate (agricultural lime grade) to increase the soil pH from its initial measured pH of 5.8 to a value within the range specified by the OECD protocol and closer to that of the Kettering loam. The OECD soil was selected to facilitate comparison with the many other ecotoxicology tests conducted with this soil (Feng et al. 2015).
Rice husk and wheat straw biochars were purchased from the UK Biochar Research Centre, Edinburgh, UK. Both biochars had been produced by pyrolysis at 550 °C and were selected because they are ‘mid-range’ in terms of the pyrolysis temperature at which biochars are generally made and thus can be considered in some respects to be representative of a range of commonly produced biochars. Also, their feedstocks are widely available agricultural waste products and so are the kinds of materials likely to be used in soil remediation and recycling/ environmental management schemes employing biochar applications. Before use in experiments, the biochars were ground into a fine powder (< 1 mm) using a mortar and pestle. The pH of the biochars (determined in 1:5 solid/deionised water slurries) was 10 and 10.5 for wheat straw and rice husk, respectively, and thus were alkaline as is typically reported for similar biochars (Beesley and Marmiroli 2011). A visual inspection of biochar surfaces was conducted through examination under a Hitachi TM-3000 scanning electron microscope (SEM) after further finely grinding subsamples and compressing into pellets and mounting on a stub using Leit-C conducting carbon cement. The SEM scans were conducted at ×500, ×1000, ×2500 and ×5000 magnification.
The organic matter content (OM%), pH and water holding capacity (WHC) of the soils and the soil + biochar treatments (described in later sections) were determined, with OM% measured by loss on ignition at 450 °C and pH measured in 1:5 solid/deionised water suspensions using a JENWAY 3510 glass pH electrode probe and meter. Soil WHC was measured by fully saturating 100 g with 100 mL deionised water, then allowing it to drain until all dripping stopped and the amount of liquid remaining in the soil calculated.
Earthworms
Lumbricus terrestris and Eisenia fetida were purchased from Yorkshire Worms (www.yorkshire-worms.co.uk). Field collection of earthworms was decided against because of (i) the large number required (> 1000 individuals) and the time and labour that would be involved in their collection, (ii) the greater genetic and physical attribute consistency within a population of hand-reared organisms compared with field collected specimens, (iii) the risk of misidentification when dealing with large numbers and (iv) the potential for differing previous land management practices (including pesticide use) across any fields sampled that may influence earthworm behaviour and survival during the ecotox assays. Between acquisition and deployment in the assays, E. fetida were maintained in a moistened substrate of bonsai compost, coir fibre and peat, whereas L. terrestris were kept in a clean commercial topsoil mixed with peat. Earthworm cultures received additional feeding of ground oats and, occasionally, lettuce leaves.
Earthworm avoidance assay
Avoidance assays were conducted with E. fetida according to the two-chamber method stipulated under ISO protocol 17512-1 (ISO 2008). The test vessels used had dimensions 15 × 15 × 10 cm (height × length × depth) and were equipped with removable vertical central partitions that divided them into two equal chambers (Howells et al. 2018). Into each vessel, 250 g non-amended (i.e. untreated) soil was placed in one chamber and an equal mass of treated soil was placed in the other. Control vessels, with untreated soil in both chambers, were also established. Before placement in the vessels, the soils had been moistened to 60% WHC. The treatments imposed on each soil were 5%, 10%, 15% and 20% biochar (w/w; n = 3), intended to reflect heavy biochar addition rates tested elsewhere (Li et al. 2011; Major et al. 2010), and that may be implemented in soil remediation and restoration efforts (Kosolsaksakul et al. 2018).
Upon commencement of the assay, the central partitions were removed and ten adult earthworms with visible clitellum introduced. A perforated transparent cover was fitted to prevent escape, and the vessels were left for 48 h after which the partitions were re-inserted and the soils removed and the number of earthworms present in each chamber counted. Avoidance behaviour was expressed in terms of the percentage of the earthworms found in the control soil chamber (Eq. 1).
Earthworm survival and development (mean mass change)
The effects of biochar application on earthworm survival and development (mass gain or loss) were examined following OECD protocol 222 (OECD 2016), using both E. fetida and L. terrestris (separately) in each of the test soils. Biochar application rates of 0%, 10% and 20% (w/w) were imposed (n = 3), with all soils and soil + biochar treatments moistened to 60–70% WHC. Plastic pots (660-mL capacity) were used as test vessels, and these were wrapped in aluminium foil to prevent lateral intrusion of light (Hund-Rinke and Wiechering 2001). The mass of soil or soil + biochar placed in the pots was equivalent to 250 g dry material. Five adult earthworms (visible clitellum) that had been rinsed with deionised water, patted dry with paper towelling and weighed were introduced to each pot. Approximately 2.5 g ground oatmeal was added to the surface of each pot to serve as food source, with a further serving provided once a week thereafter. After 14 days, the soil and earthworms were temporarily removed from their pots to facilitate earthworm survival counts and mass change determination after rinsing and drying of the earthworms. The soil and earthworms were then returned to the pots for a further 14 days, after which the final survival count and mass change measurements were recorded. Verification of survival was achieved through gentle physical stimuli with a blunt object (a pencil), and any signs of physical damage in the earthworms were noted.
At completion of the assay, the E. fetida specimens were further examined to investigate any impacts of biochar addition on earthworm moisture content. To achieve this, the E. fetida were maintained on moist filter paper for 24 h to allow depuration (Arnold and Hodson 2007) and were then rinsed in deionised water, euthanised by freezing, dried in an oven and the dry mass recorded.
An attempt was also made to examine how biochar addition affected water-soluble anions in treated soils, specifically chloride, fluoride and phosphate concentrations, to determine whether any such effects correlated with earthworm behavioural or physical effects observed. To do this, Kettering loam soils from the survival assay with L. terrestris were used to generate simulated porewater (Ardestani and van Gestel 2013; Ma et al. 2006) by saturating 25 g of recovered soil with 20 mL deionised water for 72 h before centrifugation for 20 min and filtration of the supernatant through 0.45-μm syringe filters. The filtered supernatants were then analysed by ion chromatography (Dionex ICS 1000) using certified reference solutions for construction of calibration curves.
Statistical analysis
The data were examined for statistical differences amongst treatments using analysis of variance (ANOVA), t tests and, in cases where data were not normally distributed, Mann-Whitney and Kruskal-Wallis tests. All statistical tests were conducted using Minitab software.
Results and discussion
Soil and biochar properties
The pH of the Kettering loam and artificial OECD soil was well matched, both having values measured at ~ 7.6 (Table 1). Addition of rice biochar had negligible influence on soil pH in either soil whereas addition of wheat biochar substantially increased soil pH, particularly at the 20% w/w addition rate and especially in the OECD soil where the pH rose above 9.1 (Table 1). Biochar addition also substantially increased the WHC of the soils, increasing it by ~ 50% at the highest rate applied (Table 1). The organic matter content measurements confirmed anticipated values of 6.13% ± 0.08% for Kettering loam and 15.1% ± 0.74% for the OECD soil. Scans under SEM suggested that wheat biochar had a more defined pore structure than that of the rice biochar (Supplementary Information Figs. S1 and S2).
Earthworm avoidance
In compliance with the validity criteria for the test protocol, no avoidance behaviour was exhibited in the controls of the avoidance assay with E. fetida (Fig. 1). A linear trend of avoidance was apparent for OECD soil amended with wheat biochar (i.e. linear equation: Avoidance % = 1.67 × biochar % − 0.467; R2 0.958), with the 33% avoidance maximum exhibited at the highest treatment level imposed being statistically significant in terms of difference from the control (t test t > 0, p = 0.039, Fig. 1). The other treatment/ soil combinations showed little pattern, exhibiting considerable intra-replicate variability. A much more pronounced avoidance behaviour by E. fetida was reported by Li et al. (2011) when biochar produced from apple wood sawdust was added at 10% and 20% (w/w) to a soil closely matching the OECD soil used in the present study, indicating that biochar of differing feedstocks and production conditions can have differing impacts on earthworm behaviour. The avoidance behaviour observed here was also less pronounced than that described for E. fetida introduced to a soil amended with 20% (w/w) aluminium water treatment residuals, for which an avoidance rate of ~ 50% was reported (Howells et al. 2018).
Earthworm survival
After 2 weeks of exposure, there were no impacts on survival at any of the biochar treatment levels for either of the earthworm species tested (Figs. 2 and 3). By 4 weeks, there appeared to be an effect in the 20% wheat biochar treatment in the OECD soil for L. terrestris; however, due to the sample size and high intra-replicate variability in that treatment (replicates had values of 0%, 60% and 0% survival), the reduction was not quite identified as being significantly different from the control (p = 0.087). The 20% wheat treatment in the Kettering loam soil also produced replicates with considerable variability (Fig. 2), but overall, the result for that treatment was not significantly different from the control. A comparable pattern was observed for E. fetida, with an apparent reduction after 4 weeks of exposure in the OECD soil + 20% wheat treatment (Fig. 3). However, high intra-replicate variability for this treatment (replicates of 0%, 60% and 100% survival) meant that statistically significant differences from the control were not identified. In Kettering loam soil, the 20% rice biochar application had a lower mean survival percentage for E. fetida (Fig. 3), but again, high variability within this treatment (replicates with 0%, 100% and 0%) made identification of statistically significant differences impossible. A greater number of replicates would have addressed this issue; hence, a recommendation can be made for future research involving earthworm survival studies that at least four replicates per treatment be maintained in order to raise the statistical power of the test. Nevertheless, the data generated do suggest that the 20% biochar application rates applied are on the cusp of reaching a threshold value where significant effects might occur; such an inference would be in keeping with the results reported by Anyanwu et al. (2018), who tested the effects of rice husk biochar applications on Eudrilus eugeniae (an epigeic earthworm species comparable to E. fetida) and found that statistically significant effects on survival occurred at applications of 25% and 50% w/w but not at 10%. Liesch et al. (2010) also found no significant effects on survival of E. fetida at application rates of pine chip biochar equivalent to 10% w/w. However, the Liesch et al. study did report effects in treatments with biochar generated from poultry litter even at modest rates (~ 5% w/w), indicating that biochars from different feedstocks can have differing thresholds for effects on earthworm survival.
The wide variability in survival between the replicates of some of the high biochar application rate treatments was also reflected in the physical condition observations made, as in multiple replicates across the high biochar addition treatments there were individual earthworms that appeared badly damaged (Fig. 4). The level of damage was inconsistent within and between replicates, making it difficult to draw definitive conclusions. Nevertheless, there were clearly some serious adverse effects evident that have not been widely reported in the literature. One previous study (Malev et al. 2016), however, did similarly find physical damage to Eisenia andrei earthworms exposed to high, but agronomically feasible, soil applications of biochars generated from wine tree cuttings and hardwood feedstocks, with the earthworms having developed a lumpy and irregular shape and darker coloration. The physical damage may have been caused by internal or external abrasion caused by biochar particles, and the elevated soil pH resulting from high biochar applications may have also been a factor. Other possibilities should also be considered, even if the parameters were not measured in this study and so no evidence can be presented; for example, it has been found that biochar addition can raise polycyclic aromatic hydrocarbon (PAH) concentrations in treated soils and in earthworms residing in them (Malev et al. 2016), which can have a direct toxic effect. Further research is needed to determine the processes and mechanisms responsible for the physical damage.
Earthworm development (mass change)
For L. terrestris, wheat biochar additions to OECD soil resulted in significant mass loss (i.e. loss of condition) at both 10% and 20% application rates, and this was consistent at both the 2 and 4-week stage (Fig. 5). Rice biochar addition to the OECD soil did not produce results significantly different from the untreated controls; however, there was considerable variability in the controls of the rice biochar addition treatments that made any subtle effects difficult to detect (Fig. 5). In Kettering loam, the 20% application rates for both wheat and rice biochar treatments reduced mean mass after 2 weeks (Fig. 5), whereas after 4 weeks, the differences were only statistically significant for the 20% wheat biochar treatment. The development (mass change) results for L. terrestris indicate that this is a much more sensitive assay than the survival test, i.e. it clearly identified statistically significant effect thresholds within the biochar application rates tested whereas the survival assays were only able to provide indicative values for tipping points. This is an important conclusion and should be taken into account when ecotoxicology studies are planned and conducted with an aim to assess the effects of soil amendments such as biochar on earthworms.
For E. fetida, none of the treatments in OECD soil had detectable statistically significant effects on mean mass, but there was an apparent trend towards a reduction at the 4-week stage in the 20% biochar treatments (Fig. 6). In Kettering loam, after 2 weeks, significant reductions in mean mass were observed in the 20% rice biochar treatment (Fig. 6). The effect appeared to remain consistent for that treatment after 4 weeks, but this could not be verified statistically because only one replicate pot from this treatment had surviving earthworms to determine mean mass for (see survival results above). There was an unexpected reduction after 4 weeks in the mean mass of the control E. fetida earthworms for the wheat biochar treatments in Kettering loam (Fig. 6) which, together with the wide variability in the other wheat biochar treatment results in this soil at the 4 week point, makes further interpretation difficult. The reductions in mean mass observed for earthworms in some of the biochar treatments support earlier findings, e.g. Li et al. (2011) found that 10% and 20% biochar additions caused significantly more weight loss than that observed in control soils (earthworms were not fed during that study), while Gomez-Eyles et al. (2011) found that 10% w/w additions of deciduous hardwood-derived biochar also caused significantly greater weight loss in E. fetida compared with untreated soil at both exposure time periods assessed (28 days and 56 days).
Earthworm (E. fetida) moisture content was remarkably consistent across all treatments at the end of the 4-week experiment (surviving individuals assessed only). Despite differences between treatments and replicates in terms of number of survivors, mass gain/loss and visually inspected condition, all survivors had a moisture content of ~ 82% (Table 2). This is in complete agreement with the findings of Hartenstein et al. (1980) who determined that, independently of size or live mass, moisture content in the E. fetida they examined was 81.8% ± 7.7%. This indicates that, while moisture content is essential, it is not a sensitive measure of stress or health in E. fetida because the species appears to have a very strong capacity for moisture content homeostasis. It would be interesting to determine whether this was also the case for L. terrestris.
Soluble anions in simulated soil porewater
Addition of rice biochar to the Kettering loam soil had a strong, significant effect on the soluble chloride determined in simulated porewaters generated following the survival assay. At both application rates imposed, rice biochar increased the chloride concentration 2 to 3-fold (Table 3). Wheat biochar also increased the chloride concentration, but there was much more variability amongst the replicates of the wheat biochar treatments. None of the biochar treatments affected the fluoride concentrations; however, the phosphate concentration was greatly increased (~ 100-fold) in the 20% application rate of each biochar type. The observation that both wheat and rice biochars increased the water-soluble chloride and phosphate in treated soils but that significant reductions in mass of earthworms were only noted in wheat biochar treatments (and only at 20% application rate) indicates that the increase in soluble chloride and phosphate did not in itself directly impact upon the earthworms (i.e. otherwise, effects would have been observed in both cases, if the increased soluble anions were a causative factor). Nevertheless, the effects on chloride concentrations are important because it is well known that chloride ions, when in sufficient abundance, can increase the mobility of toxic elements such as Cd that may be present in the soil (Smolders and McLaughlin 1996). This will be a particularly important consideration to take into account for scenarios in which biochar is used to remediate contaminated soils (Beesley et al. 2011; Kosolsaksakul et al. 2018). The effect on salinity (and electrical conductivity) associated with increased chloride concentrations is also important to consider because this can impact the suitability of the soil environment for microbes, plants and soil fauna. Any change to the concentration of phosphate in soil porewater is very important in terms of plant fertility and primary productivity; hence, the significant increases observed here in the 20% biochar application rates warrant further exploration. This includes examination of negative aspects, because as well as being a potential positive, any increase in soluble phosphate in biochar-treated soils could also be a potential cause for concern in terms of possible increased eutrophication risk to nearby water bodies. It is well established that addition of biochar can affect P and N cycles in treated soils by stimulating microbial activity and providing reactive surfaces upon which exchange processes can occur; however, the extent and direction of effects are highly variable and are dependent upon soil-biochar interactions dictated by the specific soils and biochars involved (Gul and Whalen 2016). Mukherjee and Zimmerman (2013) found that P release from biochars was linked to biochar volatile matter and ash content as well as functional group density. Therefore, the increased phosphate concentrations observed here in porewaters of treated soil may be linked to constituents of the biochars themselves and/or to accelerated microbial activity and greater microbial diversity following biochar addition that can influence nutrient availability, as has been noted and discussed elsewhere (Lehmann et al. 2011; Xu et al. 2016).
Conclusions
High rates of biochar addition to OECD artificial soil and to Kettering loam, a natural soil, induced a subtle level of avoidance behaviour. Effects on survival over a 4-week period were inconsistent, but death and physical damage to some individual earthworms were apparent, and the mechanisms and processes leading to these effects should be investigated further. Earthworm development (mean mass change over time) proved to be a more sensitive measure, revealing negative effects on L. terrestris at 10% and 20% (w/w) wheat biochar applications in OECD soil and at 20% (w/w) applications of both biochars tested in Kettering loam. The moisture content of E. fetida remained remarkably consistent across treatments, indicating that this is not a sensitive measure of effects. The high rates of biochar application resulted in increased water-soluble chloride and phosphate concentrations in simulated soil porewater, both of which could have significant influence on plant growth, microbial activity, invertebrate diversity and nutrient mobility and thus warrant further investigation.
References
Anyanwu IN, Alo MN, Onyekwere AM, Crosse JD, Nworie O, Chamba EB (2018) Influence of biochar aged in acidic soil on ecosystem engineers and two tropical agricultural plants. Ecotoxicol Environ Saf 153:116–126
Ardestani MM, van Gestel CAM (2013) Using a toxicokinetics approach to explain the effect of soil pH on cadmium bioavailability to Folsomia candida. Environ Pollut 180:122–130
Arnold RE, Hodson ME (2007) Effect of time and mode of depuration on tissue copper concentrations of the earthworms Eisenia andrei, Lumbricus rubellus and Lumbricus terrestris. Environ Pollut 148:21–30
Beesley L, Marmiroli M (2011) The immobilisation and retention of soluble arsenic, cadmium and zinc by biochar. Environ Pollut 159:474–480
Beesley L, Moreno-Jimenez E, Gomez-Eyles JL, Harris E, Robinson B, Sizmur T (2011) A review of biochars’ potential role in the remediation, revegetation and restoration of contaminated soils. Environ Pollut 159:3269–3282
Brami C, Glover AR, Butt KR, Lowe CN (2017) Avoidance, biomass and survival response of soil dwelling (endogeic) earthworms to OECD artificial soil: potential implications for earthworm ecotoxicology. Ecotoxicology 26:576–579
Brinza L, Schofield PF, Mosselmans JFW, Donner E, Lombi E, Paterson D, Hodson ME (2014) Can earthworm-secreted calcium carbonate immobilise Zn in contaminated soils? Soil Biol Biochem 74:1–10
Darwin CR (1881) The formation of vegetable mould through the action of worms, with observations on their habits. John Murray, London
Davies NA, Hodson ME, Black S (2003) Is the OECD acute worm toxicity test environmentally relevant? The effect of mineral form on calculated lead toxicity. Environ Pollut 121:49–54
Feng L, Zhang L, Zhang YN, Zhang P, Jiang HY (2015) Inhibition and recovery of biomarkers of earthworm Eisenia fetida after exposure to thiacloprid. Environ Sci Pollut Res 22:9475–9482
Gomez-Eyles JL, Sizmur T, Collins CD, Hodson ME (2011) Effects of biochar and the earthworm Eisenia fetida on the bioavailability of polycyclic aromatic hydrocarbons and potentially toxic elements. Environ Pollut 159:616–622
Gul S, Whalen JK (2016) Biochemical cycling of nitrogen and phosphorus in biochar-amended soils. Soil Biol Biochem 103:1–15
Hartenstein R, Leaf AL, Neuhauser EF, Bickelhaupt DH (1980) Composition of the earthworm Eisenia foetida (Savigny) and assimilation of 15 elements from sludge during growth. Comp Biochem Physiol C Pharmacol Toxicol Endocrinol 66:187–192
Houben D, Evrard L, Sonnet P (2013) Mobility, bioavailability and pH-dependent leaching of cadmium, zinc and lead in a contaminated soil amended with biochar. Chemosphere 92:1450–1457
Howells AP, Lewis SJ, Beard DB, Oliver IW (2018) Water treatment residuals as soil amendments: examining element extractability, soil porewater concentrations and effects on earthworm behaviour and survival. Ecotoxicol Environ Saf 162:334–340
Huang M, Yang L, Qin H, Jiang L, Zou Y (2013) Quantifying the effect of biochar amendment on soil quality and crop productivity in Chinese rice paddies. Field Crop Res 154:172–177
Hund-Rinke K, Wiechering H (2001) Earthworm avoidance test for soil assessments. J Soils Sediments 1:15–20
International Organization for Standardization (ISO) (2008) ISO 17512-1:2008 Soil quality - Avoidance test for determining the quality of soils and effects of chemicals on behaviour - part 1: test with earthworms (Eisenia fetida and Eisenia andrei)
Kosolsaksakul P, Oliver IW, Graham MC (2018) Evaluating cadmium bioavailability in contaminated rice paddy soils and assessing potential for contaminant immobilisation with biochar. J Environ Manag 215:49–56
Langdon CJ, Piearce TG, Meharg AA, Semple KT (2003) Inherited resistance to arsenate toxicity in two populations of Lumbricus rubellus. Environ Toxicol Chem 22:2344–2348
Lehmann J, Joseph S (2009) Biochar for environmental management. In: Lehmann J, Joseph S (eds) Biochar for Environmental Management: Science and Technology. Routledge, London
Lehmann J, Rillig MC, Thies J, Masiello CA, Hockaday WC, Crowley D (2011) Biochar effects on soil biota—a review. Soil Biol Biochem 43:1812–1836
Li D, Hockaday WC, Masiello CA, Alvarez PJJ (2011) Earthworm avoidance of biochar can be mitigated by wetting. Soil Biol Biochem 43:1732–1737
Liesch AM, Weyers SL, Gaskin JW, Das KC (2010) Impact of two different biochars on earthworm growth and survival. Ann Environ Sci 4:1–9
Lone AH, Najar GR, Ganie MA, Sofi JA, Ali T (2015) Biochar for sustainable soil health: a review of prospects and concerns. Pedosphere 25:639–653
Lowe CN, Butt KR (2005) Culture techniques for soil dwelling earthworms: a review. Pedobiologia 49:401–413
Lowe CN, Butt KR, Cheynier KY-M (2016) Assessment of avoidance behaviour by earthworms (Lumbricus rubellus and Octolasion cyaneum) in linear pollution gradients. Ecotoxicol Environ Saf 124:324–328
Ma YB, Lombi E, Oliver IW, Nolan AL, McLaughlin MJ (2006) Long-term aging of copper added to soils. Environ Sci Technol 40:6310–6317
Major J, Lehmann J, Rondon M, Goodale C (2010) Fate of soil-applied black carbon: downward migration, leaching and soil respiration. Glob Chang Biol 16:1366–1379
Malev O, Contin M, Licen S, Barbieri P, De Nobili M (2016) Bioaccumulation of polycyclic aromatic hydrocarbons and survival of earthworms (Eisenia andrei) exposed to biochar amended soils. Environ Sci Pollut Res 23:3491–3502
McHenry MP (2009) Agricultural bio-char production, renewable energy generation and farm carbon sequestration in Western Australia: certainty, uncertainty and risk. Agric Ecosyst Environ 129:1–7
Mukherjee A, Zimmerman AR (2013) Organic carbon and nutrient release from a range of laboratory-produced biochars and biochar-soil mixtures. Geoderma 193:122–130
OECD (2016) Test No. 222: Earthworm reproduction test (Eisenia fetida/Eisenia andrei), OECD guidelines for the testing of chemicals. OECD Publishing, Paris. https://doi.org/10.1787/9789264264496-en
Rinklebe J, Shaheen SM, Frohne T (2016) Amendment of biochar reduces the release of toxic elements under dynamic redox conditions in a contaminated floodplain soil. Chemosphere 142:41–47
Smolders E, McLaughlin MJ (1996) Chloride increases cadmium uptake in swiss chard in a resin-buffered nutrient solution. Soil Sci Soc Am J 60:1443–1447
Weyers SL, Spokas KA (2011) Impact of biochar on earthworm populations: a review. Appl Environ Soil Sci 2011. https://doi.org/10.1155/2011/541592
Xu N, Tan GC, Wang HY, Gai XP (2016) Effect of biochar additions to soil on nitrogen leaching, microbial biomass and bacterial community structure. Eur J Soil Biol 74:1–8
Acknowledgements
The authors would like to thank Ian Wilshaw for assistance with Dionex ion chromatography analysis and Adam Jeffery for assistance with SEM use.
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Elliston, T., Oliver, I.W. Ecotoxicological assessments of biochar additions to soil employing earthworm species Eisenia fetida and Lumbricus terrestris. Environ Sci Pollut Res 27, 33410–33418 (2020). https://doi.org/10.1007/s11356-019-04542-2
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DOI: https://doi.org/10.1007/s11356-019-04542-2